Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome 2:26680942 (forward strand) | View in location tab

Most severe consequence
Clinical significance

Synonyms

LSDB 12105

This variation has 8 HGVS names - click the plus to show

2:g.26680942G>C
ENST00000403946.3:c.5960C>G
ENSP00000385255.3:p.Pro1987Arg
ENST00000338581.6:c.*164C>G
ENST00000339598.3:c.3659C>G
ENSP00000344521.3:p.Pro1220Arg
ENST00000272371.2:c.*164C>G
ENST00000402415.3:c.*164C>G

Variation displays